Labetalol hydrochloride

Product NDC

60760-291

11-digit product format

607600291

Labeler code

60760

Product ID

60760-291_77e6083f-794b-5fa1-e053-2991aa0a9488

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Labetalol hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA075133

Marketing category

ANDA

Marketing start

2014-01-30

Marketing end

2019-10-31

Substance

LABETALOL HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record